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For 503A pharmacies, FDA reiterated a limited enforcement policy from its 2018 guidance, Compounded Drug Products That Are Essentially Copies of a Commercially Available Drug Product Under Section 503A of the Federal Food, Drug, and Cosmetic Act: the agency does not intend to take action where a compounder fills four or fewer prescriptions per calendar month of a drug that is essentially a copy of a commercially available drug

A healthcare provider will recommend the best plan

Antioxidants & Redox Signaling, 8 (56), 753762

1 This comes as Novo Nordisk and Eli Lilly continue to aggressively challenge compounded versions of their GLP-1 medications

Essential baseline evaluations include thyroid function, amylase and lipase levels, renal function, and imaging if history of thyroid disease exists